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Neurology
Developed by Roger L. Weir, M.D.
Associate Professor of Neurology
OUTLINE
1. HISTORY AND PHYSICAL
2. TECHNIQUE
Courtesy
Routine
Actual / Practice
* INTEREST
DIAGNOSIS
TREATMENT
(PREVENTION)
COUNSELLING
N common disorders
uncommon disorders
NEUROLOGICAL HISTORY
C/C or Presenting Illness (NP vs Consult)
(see below)
HPI (see below)
PMH
includes tests done
risk factors,
HTN, Diab M.,Dyslipidemia
Head trauma, auto-accident
previous surgery
c/c contd
DIZZINESS. Vertigo, tinnitus, double
vision, faintness, ataxia, inducer, reliever,
rising, flat, turning in bed, hearing.
NUMBNESS OF HAND. Which fingers,
neck pain
DIFFICULTY WALKING. Pain, where pain
DIFFICULTY SPEAKING. Understanding,
being understood
c/c contd.
BLURRED/DOUBLE VISION one or two,
in which plane,
SEEING THINGS. ?hearing voices,
threats, delusions, crawling in skin, drug
use, FH.
Neurological History
FAMILY HISTORY
Risk factors suggested
Sickle Cell anemia
Muscular Dystrophy
Myocardial Infarction
Spinocerebellar degeneration
Neurological History
SOCIAL HISTORY
Alcoholism, Cocaine use
Nicotine use,
Occupation
Living situation
Spousal/emotional status
ROS
THE NEUROLOGICAL
EXAMINATION
MENTATION AND SPEECH
CRANIAL NERVES (2 to 12)
MOTOR FUNCTION
(Normal, Impaired, Abnormal movement)
Memory:
Digit span (reverse versus forward), recent, remote, fund of
information
Calculations:
Arithmetic, money (?education)
Draw a clock
Draw a person
Copy a figure
Confusion
Denial / Inattention
Anosognosia
Apraxia
Distractibility
Hallucinations:
Auditory, visual, other
Mood:
anxiety, depression
Appropriateness of interaction
Following Commands:
Verbal, written, gestures
Naming
Repetition:
sentence, word, counting, singing
Reading
Writing:
spontaneously, copying,
Calculations / arithmetic
CRANIAL NERVES
1. 2*. 3*. 4. 5. 6*, 7*, 8*, 9, 10, 11, 12
CRANIAL NERVES
1. 2*. 3*. 4. 5. 6*, 7*, 8*, 9, 10, 11, 12
*CN7:
Brow elevation, eyelid closure, smile
facial droop +autonomic/sensory
*CN8: Auditory acuity, dizziness, balance,
tinnitus, nystagmus, Weber, Rinne
CN9: Gag reflex, swallowing
CN10: Vocal cord movement + autonomic
CN11: Sternocleido-Mastoid, Trapezius
CN12: Tongue deviation, atrophy, fasciculations
MOTOR EXAMINATION
WASTING / HYPERTROPHY
(Duchenne muscular
dystrophy)
FASCICULATIONS (evidence of lower
motor neuron dysfunction)
MOTOR EXAMINATION
STRENGTH:
Proximal (characteristic of muscle problem),
distal (characteristic of periph. neuropathy),
*Right vs. Left,
upper limbs, lower limbs,
nerve root distribution,
nerve distribution,
severity(0 to 5),
pain effect,
other.
MOTOR EXAMINATION
RIGIDITY, SPASTICITY, OTHER
SPEED OF MOVEMENT
ABNORMAL INVOLUNTARY MOVEMENTS
eg tremor
COORDINATION
Cerebellar function
Reason for doing the strength test before
coordination is to know if incoordination is
due only to muscle weakness
May apparently vary with strength
COORDINATION
Cerebellar function
*FINGER / NOSE test:
*HEEL/SHIN test:
proximal, transit
ankle dorsiflexion
CHECK / REBOUND:**
POSTURE
STANDING BASE: width, stability
GAIT: stable, asymmetric, ?type
REFLEXES
SUPERFICIAL:
abdominal, cremasteric
Abdominal reflex disappears in the presence of upper motor neuron
(multiple sclerosis)
PATHOLOGICAL:
DEEP TENDON(R/L):
GRADING:
0, 1, 2 , 3, 4
where 2 represents an average reflex.
SENSATION
Touch:
Double simultaneous stimulation
Graphesthesia
Stereognosis
Two-point discrimination
Point localization
MENINGEAL SIGNS
bacterial/ viral/other meningitis
& subarachnoid hemorrhage
NECK STIFFNESS
KERNIG
BRUDZINSKI
PHOTOPHOBIA
EYEBALL TENDERNESS (least
important)
SPINE/MUSCULO-SKELETAL
Spine tenderness:
Cervical, Lumbar, Thoracic
Sacro-iliac joints
Scalp muscles
Cervical paraspinals
Lateral neck muscles
Scapular region muscles
Lumbar paraspinals
Lateral sacrum